Parkinsonian Disorders Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

43 genes associated with the Parkinsonian Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ANKK1 ankyrin repeat and kinase domain containing 1
APOE apolipoprotein E
ATP13A2 ATPase type 13A2
ATXN2 ataxin 2
ATXN3 ataxin 3
ATXN8 ataxin 8
BDNF brain-derived neurotrophic factor
BST1 bone marrow stromal cell antigen 1
C10ORF2 chromosome 10 open reading frame 2
C9ORF72 chromosome 9 open reading frame 72
COMT catechol-O-methyltransferase
CYP2D6 cytochrome P450, family 2, subfamily D, polypeptide 6
DRD2 dopamine receptor D2
DRD3 dopamine receptor D3
EIF4G1 eukaryotic translation initiation factor 4 gamma, 1
FBXO7 F-box protein 7
FMR1 fragile X mental retardation 1
FUS FUS RNA binding protein
GBA glucosidase, beta, acid
GCH1 GTP cyclohydrolase 1
GIGYF2 GRB10 interacting GYF protein 2
GRN granulin
GSK3B glycogen synthase kinase 3 beta
HFE hemochromatosis
HTR2A 5-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled
HTR2C 5-hydroxytryptamine (serotonin) receptor 2C, G protein-coupled
HTRA2 HtrA serine peptidase 2
LRRK2 leucine-rich repeat kinase 2
MAPT microtubule-associated protein tau
NR4A2 nuclear receptor subfamily 4, group A, member 2
PACRG PARK2 co-regulated
PARK2 parkin RBR E3 ubiquitin protein ligase
PARK7 parkinson protein 7
PINK1 PTEN induced putative kinase 1
PLA2G6 phospholipase A2, group VI (cytosolic, calcium-independent)
POLG polymerase (DNA directed), gamma
RGS2 regulator of G-protein signaling 2
SLC25A4 solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 4
SNCA synuclein, alpha (non A4 component of amyloid precursor)
SPR sepiapterin reductase (7,8-dihydrobiopterin:NADP+ oxidoreductase)
TBP TATA box binding protein
UCHL1 ubiquitin carboxyl-terminal esterase L1 (ubiquitin thiolesterase)
VPS35 vacuolar protein sorting 35 homolog (S. cerevisiae)